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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H16O
Molecular Weight 152.2334
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARVEOL, CIS-(-)-

SMILES

CC(=C)[C@@H]1CC=C(C)[C@H](O)C1

InChI

InChIKey=BAVONGHXFVOKBV-NXEZZACHSA-N
InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H16O
Molecular Weight 152.2334
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Distinct effects of carvone analogues on the isolated nerve of rats.
2010-10-25
Inhibitory effects of substrate and product on the carvone biotransformation activity of Rhodococcus erythropolis.
2008-07
Monoterpenoid agonists of TRPV3.
2007-06
Herbal monoterpene alcohols inhibit propofol metabolism and prolong anesthesia time.
2006-05-30
Cell adaptation to solvent, substrate and product: a successful strategy to overcome product inhibition in a bioconversion system.
2005-12
Adaptation of Rhodococcus erythropolis DCL14 to growth on n-alkanes, alcohols and terpenes.
2005-05
Monoterpene biosynthesis pathway construction in Escherichia coli.
2003-09
Monoterpene regulation of Ras and Ras-related protein expression.
2003-06
Effects of Anethum graveolens L. seed extracts on experimental gastric irritation models in mice.
2002-12-19
Metabolism of (+)- and (-)-limonenes to respective carveols and perillyl alcohols by CYP2C9 and CYP2C19 in human liver microsomes.
2002-05
Species differences in the metabolism of (+)- and (-)-limonenes and their metabolites, carveols and carvones, by cytochrome P450 enzymes in liver microsomes of mice, rats, guinea pigs, rabbits, dogs, monkeys, and humans.
2002
Degradation of pinene by Bacillus pallidus BR425.
1998
Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols.
1995-10-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:37:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:37:28 GMT 2025
Record UNII
OOZ105PLI9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2247, CIS-(-)-
Preferred Name English
CARVEOL, CIS-(-)-
Common Name English
L-CIS-CARVEOL
Common Name English
CIS-(-)-CARVEOL
Common Name English
(1R-CIS)-2-METHYL-5-ISOPROPENYL-2-CYCLOHEXEN-1-OL
Systematic Name English
2-CYCLOHEXEN-1-OL, 2-METHYL-5-(1-METHYLETHENYL)-, (1R,5R)-
Systematic Name English
(1R,5R)-(-)-CIS-CARVEOL
Common Name English
CARVEOL, L-CIS-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID701036409
Created by admin on Mon Mar 31 18:37:28 GMT 2025 , Edited by admin on Mon Mar 31 18:37:28 GMT 2025
PRIMARY
CAS
2102-59-2
Created by admin on Mon Mar 31 18:37:28 GMT 2025 , Edited by admin on Mon Mar 31 18:37:28 GMT 2025
PRIMARY
PUBCHEM
330573
Created by admin on Mon Mar 31 18:37:28 GMT 2025 , Edited by admin on Mon Mar 31 18:37:28 GMT 2025
PRIMARY
ECHA (EC/EINECS)
218-270-5
Created by admin on Mon Mar 31 18:37:28 GMT 2025 , Edited by admin on Mon Mar 31 18:37:28 GMT 2025
PRIMARY
FDA UNII
OOZ105PLI9
Created by admin on Mon Mar 31 18:37:28 GMT 2025 , Edited by admin on Mon Mar 31 18:37:28 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER